Molecular cloning, characterization and tissue expression of porcine Toll-like receptor 4

A cDNA containing the porcine Toll-like receptor 4 (TLR4) coding sequence has been cloned by RT-PCR from alveolar macrophages mRNA, and its complete sequence has been determined. The predicted amino acid sequence comprises an extracellular domain with 21 leucine-rich repeats (LRR) and a LRR-C-terminal (LRR-CT) motif, followed by a 30 amino acid transmembrane segment, and a 179 amino acid intracytoplasmic region containing the Toll/IL-1R domain. Pig TLR4 shows 63-80% amino acid sequence identity with those of cow, horse, cat, human, rabbit and mouse. The degree of sequence identity rises to over 90% in the TIR domain. The whole TLR4 sequence and its ectodomain were expressed as GFP fusion proteins in CHO cells. Using RT-PCR analysis, porcine TLR4 transcripts were detected in DCs, monocytes and macrophages, and in tissue samples of bone marrow, thymus, lymph node, spleen, brain, liver, kidney and ovary. The expressed protein will be used for the development of reagents. Knowledge of TLR4 expression will help to address mechanisms of immune induction by antigens and vaccines. © 2005 Elsevier Ltd. All rights reserved.

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Main Authors: Álvarez, B., Revilla, C., Chamorro, S., López-Fraga, M., Alonso, F., Domínguez, J., Ezquerra, A.
Format: journal article biblioteca
Language:eng
Published: 2006
Online Access:http://hdl.handle.net/20.500.12792/4848
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spelling dig-inia-es-20.500.12792-48482020-12-15T09:52:42Z Molecular cloning, characterization and tissue expression of porcine Toll-like receptor 4 Álvarez, B. Revilla, C. Chamorro, S. López-Fraga, M. Alonso, F. Domínguez, J. Ezquerra, A. A cDNA containing the porcine Toll-like receptor 4 (TLR4) coding sequence has been cloned by RT-PCR from alveolar macrophages mRNA, and its complete sequence has been determined. The predicted amino acid sequence comprises an extracellular domain with 21 leucine-rich repeats (LRR) and a LRR-C-terminal (LRR-CT) motif, followed by a 30 amino acid transmembrane segment, and a 179 amino acid intracytoplasmic region containing the Toll/IL-1R domain. Pig TLR4 shows 63-80% amino acid sequence identity with those of cow, horse, cat, human, rabbit and mouse. The degree of sequence identity rises to over 90% in the TIR domain. The whole TLR4 sequence and its ectodomain were expressed as GFP fusion proteins in CHO cells. Using RT-PCR analysis, porcine TLR4 transcripts were detected in DCs, monocytes and macrophages, and in tissue samples of bone marrow, thymus, lymph node, spleen, brain, liver, kidney and ovary. The expressed protein will be used for the development of reagents. Knowledge of TLR4 expression will help to address mechanisms of immune induction by antigens and vaccines. © 2005 Elsevier Ltd. All rights reserved. 2020-10-22T18:15:37Z 2020-10-22T18:15:37Z 2006 journal article http://hdl.handle.net/20.500.12792/4848 10.1016/j.dci.2005.06.020 eng Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ open access
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country España
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libraryname Biblioteca del INIA España
language eng
description A cDNA containing the porcine Toll-like receptor 4 (TLR4) coding sequence has been cloned by RT-PCR from alveolar macrophages mRNA, and its complete sequence has been determined. The predicted amino acid sequence comprises an extracellular domain with 21 leucine-rich repeats (LRR) and a LRR-C-terminal (LRR-CT) motif, followed by a 30 amino acid transmembrane segment, and a 179 amino acid intracytoplasmic region containing the Toll/IL-1R domain. Pig TLR4 shows 63-80% amino acid sequence identity with those of cow, horse, cat, human, rabbit and mouse. The degree of sequence identity rises to over 90% in the TIR domain. The whole TLR4 sequence and its ectodomain were expressed as GFP fusion proteins in CHO cells. Using RT-PCR analysis, porcine TLR4 transcripts were detected in DCs, monocytes and macrophages, and in tissue samples of bone marrow, thymus, lymph node, spleen, brain, liver, kidney and ovary. The expressed protein will be used for the development of reagents. Knowledge of TLR4 expression will help to address mechanisms of immune induction by antigens and vaccines. © 2005 Elsevier Ltd. All rights reserved.
format journal article
author Álvarez, B.
Revilla, C.
Chamorro, S.
López-Fraga, M.
Alonso, F.
Domínguez, J.
Ezquerra, A.
spellingShingle Álvarez, B.
Revilla, C.
Chamorro, S.
López-Fraga, M.
Alonso, F.
Domínguez, J.
Ezquerra, A.
Molecular cloning, characterization and tissue expression of porcine Toll-like receptor 4
author_facet Álvarez, B.
Revilla, C.
Chamorro, S.
López-Fraga, M.
Alonso, F.
Domínguez, J.
Ezquerra, A.
author_sort Álvarez, B.
title Molecular cloning, characterization and tissue expression of porcine Toll-like receptor 4
title_short Molecular cloning, characterization and tissue expression of porcine Toll-like receptor 4
title_full Molecular cloning, characterization and tissue expression of porcine Toll-like receptor 4
title_fullStr Molecular cloning, characterization and tissue expression of porcine Toll-like receptor 4
title_full_unstemmed Molecular cloning, characterization and tissue expression of porcine Toll-like receptor 4
title_sort molecular cloning, characterization and tissue expression of porcine toll-like receptor 4
publishDate 2006
url http://hdl.handle.net/20.500.12792/4848
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